Yen Ming Ren, Saier Milton H
Division of Biological Sciences, University of California at San Diego, La Jolla, CA 92093-0116, USA.
Prog Biophys Mol Biol. 2007 May-Jun;94(1-2):5-14. doi: 10.1016/j.pbiomolbio.2007.03.006. Epub 2007 Mar 15.
There has been some controversy as to whether vertebrate pannexins are related to invertebrate innexins. Using statistical, topological and conserved sequence motif analyses, we establish that these proteins belong to a single superfamily. We also demonstrate the occurrence of large homologues with C-terminal proline-rich domains that may have arisen by gene fusion events. Phylogenetic analyses reveal the orthologous and paralogous relationships of these homologues to each other. We show that different sets of orthologous paralogues underwent sequence divergence at markedly different rates, suggesting differential pressures through evolutionary time promoting or restricting sequence divergence. We further show that the first 2 TMS-containing halves of these homologues underwent sequence divergence more slowly than the second 2 TMS-containing halves and analyze these differences. These bioinformatic analyses should serve as useful guides for future studies of structure, function and evolutionary aspects of this important superfamily.
关于脊椎动物的泛连接蛋白是否与无脊椎动物的连接蛋白相关存在一些争议。通过统计、拓扑和保守序列基序分析,我们确定这些蛋白质属于一个单一的超家族。我们还证明了存在具有富含脯氨酸的C末端结构域的大型同源物,这些同源物可能是由基因融合事件产生的。系统发育分析揭示了这些同源物之间的直系同源和旁系同源关系。我们表明,不同组的直系同源旁系同源物以明显不同的速率发生序列分歧,这表明在进化过程中存在促进或限制序列分歧的不同压力。我们进一步表明,这些同源物的前两个含跨膜结构域(TMS)的部分比后两个含TMS的部分序列分歧更慢,并分析了这些差异。这些生物信息学分析应为该重要超家族的结构、功能和进化方面的未来研究提供有用的指导。